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A Novel Recombinant DNA Vaccine Encoding Mycobacterium Tuberculosis ESAT-6 and FL Protects Against Mycobacterium Tuberculosis Challenge in Mice

Overview
Journal J Biomed Res
Specialty General Medicine
Date 2013 Oct 3
PMID 24086174
Citations 8
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Abstract

Mycobacterium tuberculosis 6-kDa early secretory antigenic target (ESAT-6) is a dominant target antigen for cell-mediated immunity in the early phase of tuberculosis. The fms-like tyrosine kinase 3 ligand (FL) that induces potent immune response has been used as an adjuvant in vaccine development. In this study, a new recombinant plasmid (pIRES-epitope-peptides-FL) encoding three T cell epitopes of ESAT-6 and FL was constructed, and the immunogenicity of the DNA vaccine was assessed in C57BL/6 mice immunized with the plasmid DNA vaccine. Additionally, a strategy of intramuscular injection with the DNA vaccine (prime) and intranasal administration of the epitope peptides (boost) was employed to induce higher immune reaction of the mice. The results showed that mice vaccinated with the recombinant plasmid DNA vaccine and boosted with the peptides not only increased the levels of Th1 cytokines (IFN-γ and IL-12), the number of IFN-γ(+) T cells and activities of cytotoxic T lymphocytes as well as IgG, but also enhanced protection against Mycobacterium tuberculosis challenge. In conclusion, these data indicate that the novel recombinant pIRES-epitope-peptides-FL plasmid is a useful DNA vaccine for preventing Mycobacterium tuberculosis infection.

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References
1.
Djuardi Y, Sartono E, Wibowo H, Supali T, Yazdanbakhsh M . A longitudinal study of BCG vaccination in early childhood: the development of innate and adaptive immune responses. PLoS One. 2010; 5(11):e14066. PMC: 2988815. DOI: 10.1371/journal.pone.0014066. View

2.
Brodin P, Majlessi L, Marsollier L, de Jonge M, Bottai D, Demangel C . Dissection of ESAT-6 system 1 of Mycobacterium tuberculosis and impact on immunogenicity and virulence. Infect Immun. 2005; 74(1):88-98. PMC: 1346617. DOI: 10.1128/IAI.74.1.88-98.2006. View

3.
Lyashchenko K, Colangeli R, Houde M, Al Jahdali H, Menzies D, Gennaro M . Heterogeneous antibody responses in tuberculosis. Infect Immun. 1998; 66(8):3936-40. PMC: 108457. DOI: 10.1128/IAI.66.8.3936-3940.1998. View

4.
Behr M, Wilson M, Gill W, Salamon H, Schoolnik G, Rane S . Comparative genomics of BCG vaccines by whole-genome DNA microarray. Science. 1999; 284(5419):1520-3. DOI: 10.1126/science.284.5419.1520. View

5.
Young D, Perkins M, Duncan K, Barry 3rd C . Confronting the scientific obstacles to global control of tuberculosis. J Clin Invest. 2008; 118(4):1255-65. PMC: 2276805. DOI: 10.1172/JCI34614. View